V. Carlton

发表

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

Steven J. Schrodi, Annette Lee, P. Gregersen, 2004, American journal of human genetics.

Immunoglobulin and T cell receptor gene high-throughput sequencing quantifies minimal residual disease in acute lymphoblastic leukemia and predicts post-transplantation relapse and survival.

V. Carlton, A. Logan, N. Vashi, 2014, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

High-throughput method for analyzing methylation of CpGs in targeted genomic regions

P. Spellman, J. Gray, J. Ireland, 2010, Proceedings of the National Academy of Sciences.

Analysis of Families in the Multiple Autoimmune Disease Genetics Consortium (madgc) Collection: the Ptpn22 620w Allele Associates with Multiple Autoimmune Phenotypes

Annette Lee, P. Gregersen, Wentian Li, 2022 .

Diverse somatic mutation patterns and pathway alterations in human cancers.

David P. Davis, B. Peters, R. Bourgon, 2010, Nature.

Antigen Presentation Profiling Reveals Recognition of Lymphoma Immunoglobulin Neoantigens

Ash A. Alizadeh, Aaron M. Newman, Lisa E. Wagar, 2017, Nature.

Functional single nucleotide polymorphism-based association studies

J. Ireland, V. Carlton, M. Faham, 2006, Human Genomics.

eScholarship Title Prediction of epigenetically regulated genes in breast cancer cell lines

Leandro A. Loss, P. Spellman, J. Gray, 2010 .

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

Kristin G Ardlie, Carl D Langefeld, Monica Chang, 2004, American journal of human genetics.

Molecular basis of intrahepatic cholestasis

L. Pawlikowska, V. Carlton, L. Bull, 2004, Annals of medicine.

Nonsynonymous Coding Single-Nucleotide Polymorphisms Spanning the Genome in Relation to Glioblastoma Survival and Age at Diagnosis

M. Prados, V. Carlton, M. Moghadassi, 2007, Clinical Cancer Research.

Cancer vaccines and T cell therapy.

R. Advani, H. Kohrt, D. Czerwinski, 2013, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Detection of classical Hodgkin lymphoma specific sequence in peripheral blood using a next‐generation sequencing approach

Maria A. Rodriguez, Y. Oki, V. Carlton, 2015, British journal of haematology.

Prognostic value of sequencing-based minimal residual disease detection in patients with multiple myeloma who underwent autologous stem-cell transplantation

V. Carlton, M. Faham, K. Kong, 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

An algorithm to detect abnormal mRNA splicing and assess its clinical impact in individuals undergoing genetic testing for hereditary cancer syndromes

R. Nussbaum, Laurent Frésard, V. Carlton, 2022, bioRxiv.

The prognostic value of the depth of response in multiple myeloma depends on the time of assessment, risk status and molecular subtype

T. Willis, B. Barlogie, G. Morgan, 2017, Haematologica.

Next-generation sequencing and real-time quantitative PCR for minimal residual disease detection in B-cell disorders

A. Palumbo, V. Carlton, F. Pépin, 2014, Leukemia.

Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC

N. Freimer, R. Sinke, D. Barton, 1999, Human Genetics.

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC‐1] and Byler syndrome): Evidence for heterogeneity

N. Freimer, V. Carlton, K. Setchell, 1997, Hepatology.

Minimal residual disease negativity using deep sequencing is a major prognostic factor in multiple myeloma.

T. Willis, B. Pégourié, P. Richardson, 2018, Blood.

Prediction of epigenetically regulated genes in breast cancer cell lines

Bahram Parvin, Paul T. Spellman, Steffen Durinck, 2010, BMC Bioinformatics.

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

W. Lim, E. Puffenberger, K. Strauss, 2003, Nature Genetics.

High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays

P. Spellman, G. Mills, J. Gray, 2009, BMC Medical Genomics.

A comparison of minimal residual disease detection in autografts among ASO‐qPCR, droplet digital PCR, and next‐generation sequencing in patients with multiple myeloma who underwent autologous stem cell transplantation

V. Carlton, M. Faham, K. Kong, 2018, British journal of haematology.

Next-Generation Sequencing Reveals Clonal Evolution at the Immunoglobulin Loci in Chronic Lymphocytic Leukemia

V. Carlton, A. Logan, M. Faham, 2014 .

Massive evolution of the immunoglobulin heavy chain locus in children with B precursor acute lymphoblastic leukemia.

V. Carlton, F. Pépin, A. Logan, 2012, Blood.

Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD)

Martin Moorhead, Malek Faham, Eugeni Namsaraev, 2008, Human mutation.

Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups

P. Hardenbol, T. Willis, J. Ireland, 2006, Human Genetics.

Minimal residual disease quantification using consensus primers and high-throughput IGH sequencing predicts post-transplant relapse in chronic lymphocytic leukemia

B. Narasimhan, V. Carlton, A. Logan, 2013, Leukemia.

Deep-sequencing approach for minimal residual disease detection in acute lymphoblastic leukemia.

D. Campana, C. Pui, V. Carlton, 2012, Blood.

Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region.

N. Freimer, V. Carlton, A. Knisely, 1995, Human molecular genetics.

Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome.

F. Kronenberg, V. Carlton, R. Margreiter, 2003, The Journal of pediatrics.

Highly efficient somatic-mutation identification using Escherichia coli mismatch-repair detection

B. Peters, Peter Hong, Z. Kan, 2007, Nature Methods.

PTPN 22 genetic variation : evidence for multiple variants associated with rheumatoid arthritis

Steven J. Schrodi, P. Gregersen, E. Beasley, 2016 .

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

Steven J. Schrodi, P. Gregersen, E. Beasley, 2005, American journal of human genetics.

Genetic Variation : Evidence for Multiple Variants Associated with Rheumatoid Arthritis

Steven J. Schrodi, P. Gregersen, E. Beasley, 2005 .

The prognostic value of clonal heterogeneity and quantitative assessment of plasma circulating clonal IG-VDJ sequences at diagnosis in patients with follicular lymphoma

F. Jardin, G. Salles, V. Carlton, 2017, Oncotarget.

Next‐generation sequencing‐based detection of circulating tumour DNA After allogeneic stem cell transplantation for lymphoma

V. Carlton, J. Ritz, M. Faham, 2016, British journal of haematology.

Deep B and T Cell Repertoire Sequencing to Evaluate Minimal Residual Disease and T Cell Responses in a Therapeutic Vaccine Trial for Mantle Cell Lymphoma

R. Advani, H. Kohrt, D. Czerwinski, 2012 .

Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64

N. Freimer, T. Delhaas, R. Sinke, 1997, Human Genetics.

Impaired B Cell Clonotype Diversification After Allogeneic Hematopoietic Cell Transplantation Predicts Graft-Versus-Host Disease

V. Carlton, A. Logan, M. Faham, 2013 .

Discovery of T Cell Receptor β Motifs Specific to HLA–B27–Positive Ankylosing Spondylitis by Deep Repertoire Sequence Analysis

James Ireland, Francois Pepin, Martin Moorhead, 2017, Arthritis & rheumatology.

Evaluation of Minimal Residual Disease (MRD) in Relapsed/Refractory Multiple Myeloma (RRMM) Patients Treated with Daratumumab in Combination with Lenalidomide Plus Dexamethasone or Bortezomib Plus Dexamethasone

J. Laubach, V. Carlton, T. Plesner, 2016 .

High-throughput, high-accuracy array-based resequencing

Ronald W. Davis, Joseph E. Peterson, J. Ireland, 2009, Proceedings of the National Academy of Sciences.

Antigen presentation profiling reveals T-cell recognition of lymphoma immunoglobulin neoantigens

Ash A. Alizadeh, Mark M. Davis, Michael R. Green, 2016, The Journal of Immunology.

Deep Sequencing Reveals Oligoclonality At The Immunoglobulin Locus In Multiple Myeloma Patients

V. Carlton, M. Faham, M. Moorhead, 2013 .

Highly Sensitive Detection of Minimal Residual Disease in Acute Lymphoblastic Leukemia Using Next-Generation Sequencing of Immunoglobulin Heavy Chain Variable Region

D. Campana, T. Willis, V. Carlton, 2011 .

A Genomic-Profile Derived Summary Measure of Chromosomal Breakpoints Predicts Response to Treatment with the DNA-Damaging Agent Cisplatin.

Z. Szallasi, A. Eklund, Qiyuan Li, 2009 .

Minimal Residual Disease Quantification in Acute Lymphoblastic Leukemia Using High-Throughput Sequencing of Multiple Immunoreceptor Genes Predicts Relapse and Survival After Allogeneic Hematopoietic Cell Transplantation.

T. Willis, V. Carlton, A. Logan, 2012 .

High-Throughput Immunoglobulin Gene Sequencing Quantifies Minimal Residual Disease in CLL with 10e-6 Sensitivity and Strongly Predicts Relapse After Allogeneic Hematopoietic Cell Transplantation

T. Willis, V. Carlton, A. Logan, 2011 .

Association of the PTPN22 C1858T single-nucleotide polymorphism with rheumatoid arthritis phenotypes in an inception cohort.

A. Begovich, V. Carlton, A. Chokkalingam, 2005, Arthritis and rheumatism.

Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.

Annette Lee, P. Gregersen, Wentian Li, 2005, American journal of human genetics.

Cancer vaccines and T cell therapy.

R. Advani, H. Kohrt, D. Czerwinski, 2013, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.